Allele Registry

Canonical Allele Identifier: PA2825131086

Gene: SCN5A HGNC NCBI

ClinVar Allele:

1348276

ClinVar RCV:

RCV003657351

ClinVar Variation:

1356845

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Gly1261Cys	CA352149068 NM_000335.5:c.3781G>T