Annotation Detail
Information
- Associated Genes
- VWF
- Associated Variants
-
VWF p.Arg1205Leu (p.R1205L)
(
ENST00000261405.10 )
VWF p.Arg1205Leu (p.R1205L) ( ENST00000261405.10 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000552.5(VWF):c.3614G>T (p.Arg1205Leu) AND not provided
- ClinVar Allele ID
- 106148
- ClinVar RefSeq Alternation Syntax
- NM_000552.5:c.3614G>T
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000086667
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs