Allele Registry

Canonical Allele Identifier: PA218916

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_932173.1:p.Val1098Leu	CA017002 NM_198056.3:c.3292G>T CA352138792 NM_198056.3:c.3292G>C