Allele Registry

Canonical Allele Identifier: PA211839

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058446

RCV000148854

RCV000456073

RCV000987224

RCV003486629

ClinVar Variation:

67682

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Ala572Ser	CA015256 NM_001099404.2:c.1714G>T