Allele Registry

Canonical Allele Identifier: PA218844

Gene: SCN5A HGNC NCBI

ClinVar Allele:

78583

909553

ClinVar RCV:

RCV000058452

RCV001843165

RCV001876102

ClinVar Variation:

67688

923068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Asn592Lys	CA015355 NM_001099404.2:c.1776C>A CA058791 NM_001099404.2:c.1776C>G