Allele Registry

Canonical Allele Identifier: PA181449

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

24428

ClinVar RCV:

RCV000009987

RCV000058786

RCV000148848

RCV000154827

RCV000619902

RCV000766811

RCV001841236

RCV002476953

ClinVar Variation:

9389

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Arg1826His	CA019280 NM_001099404.2:c.5477G>A