Allele Registry

Canonical Allele Identifier: PA218950

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000058819

RCV000987193

RCV001143896

RCV001143897

RCV001150018

RCV001150019

RCV001150020

RCV001842400

RCV002354253

RCV003317073

ClinVar Variation:

68020

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Leu1987Arg	CA019559 NM_000335.5:c.5960T>G