Annotation Detail
Information
- Associated Genes
- HBB LOC107133510 LOC110006319
- Associated Variants
-
HBB p.Val127Ala (p.V127A)
(
ENST00000647020.1,
ENST00000335295.4 )
HBB p.Val127Ala (p.V127A) ( ENST00000335295.4, ENST00000647020.1 ) - Source Database
- ClinVar
- Description
- NM_000518.5(HBB):c.380T>C (p.Val127Ala) AND HEMOGLOBIN BEIRUT
- ClinVar Allele ID
- 30145
- ClinVar RefSeq Alternation Syntax
- NM_000518.5:c.380T>C
- Clinical Significance Description
- other
- Clinical Significance Last Update
- 2017-12-12
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000016260
- Observed Origin Sample
- germline
- Pubmed
- 3557996
- Pubmed
- 6879181
Drugs