Allele Registry

Canonical Allele Identifier: PA2825129538

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003592359

ClinVar Variation:

2774477

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Asn598Asp	CA352146143 NM_000335.5:c.1792A>G