Allele Registry

Canonical Allele Identifier: PA2825129446

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003772708

ClinVar Variation:

1393412

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Thr559Lys	CA352146777 NM_000335.5:c.1676C>A