Allele Registry

Canonical Allele Identifier: PA177829

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000058447

RCV000143951

RCV000151795

RCV000157480

RCV000157481

RCV000244195

RCV000264595

RCV000268589

RCV000326049

RCV000360867

RCV000438831

RCV000852965

RCV001094811

RCV001842295

RCV002504971

RCV003486630

ClinVar Variation:

67683

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Ala572Asp	CA015266 NM_001099404.2:c.1715C>A