Allele Registry

Canonical Allele Identifier: PA199838

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058737

RCV000171771

RCV000621882

RCV000766807

RCV001842377

ClinVar Variation:

67952

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Ala1679Thr	CA018863 NM_000335.5:c.5035G>A