Allele Registry

Canonical Allele Identifier: PA177799

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000058541

RCV000171570

RCV000766794

RCV001145179

RCV001145180

RCV001145181

RCV001145182

RCV001147136

RCV001842324

RCV003149712

RCV004019046

ClinVar Variation:

67771

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Ala997Thr	CA016710 NM_000335.5:c.2989G>A