Annotation Detail
Information
- Associated Genes
- KCNH2
- Associated Variants
-
KCNH2 p.Val822Met (p.V822M)
(
ENST00000262186.10,
ENST00000330883.9,
ENST00000713701.1,
ENST00000713710.1 )
KCNH2 p.Val822Met (p.V822M) ( ENST00000262186.10, ENST00000330883.9, ENST00000713701.1, ENST00000713710.1 ) - Associated Disease
- long QT syndrome 1
- Source Database
- ClinVar
- Description
- NM_000238.4(KCNH2):c.2464G>A (p.Val822Met) AND Long QT syndrome 1
- ClinVar Allele ID
- 29463
- ClinVar RefSeq Alternation Syntax
- NM_172057.3:c.1444G>A
- ClinVar RefSeq Alternation Syntax
- NM_000238.4:c.2464G>A
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000509399
- ClinVar Disease
- Long QT syndrome 1
- Observed Origin Sample
- unknown
Drugs