Allele Registry

Canonical Allele Identifier: PA183732

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000058543

RCV000155885

RCV000766795

RCV000987213

RCV001145176

RCV001145177

RCV001145178

RCV001149459

RCV001149460

RCV001842325

RCV002433565

ClinVar Variation:

67772

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Cys1004Arg	CA016748 NM_000335.5:c.3010T>C