Annotation Detail
Information
- Associated Genes
- VHL
- Associated Variants
-
VHL p.His191Asp (p.H191D)
(
ENST00000256474.3,
ENST00000345392.3,
ENST00000696143.2,
ENST00000696153.1,
ENST00000713811.1,
ENST00000713812.1,
ENST00000713815.1,
ENST00000713982.1 )
VHL p.Pro192Ser (p.P192S) ( ENST00000256474.3, ENST00000345392.3, ENST00000696143.2, ENST00000696153.1, ENST00000713811.1, ENST00000713812.1, ENST00000713815.1, ENST00000713982.1 )
VHL p.His191Asp (p.H191D) ( ENST00000256474.3, ENST00000345392.3, ENST00000696143.2, ENST00000696153.1, ENST00000713811.1, ENST00000713812.1, ENST00000713815.1, ENST00000713982.1 )
VHL p.Pro192Ser (p.P192S) ( ENST00000256474.3, ENST00000345392.3, ENST00000696143.2, ENST00000696153.1, ENST00000713811.1, ENST00000713812.1, ENST00000713815.1, ENST00000713982.1 ) - Associated Disease
- ERYTHROCYTOSIS, FAMILIAL, 2
- Source Database
- DisGeNET
- Description
- Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.
- Pubmed
- 12844285
- Original source reporting the Gene Disease association
- UNIPROT
- DisGENET score for the Gene Disease association
- 0.56
- Year of publication
- 2003
Drugs