Allele Registry

Canonical Allele Identifier: PA218914

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

78683

ClinVar RCV:

RCV000058561

RCV001089363

RCV001147830

RCV001147831

RCV001147832

RCV001147833

RCV001149365

RCV001149366

RCV001842331

RCV002321560

RCV003235025

ClinVar Variation:

67788

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Val1097Leu	CA017002 NM_000335.5:c.3289G>T CA352138792 NM_000335.5:c.3289G>C