Allele Registry

Canonical Allele Identifier: PA2825129454

Gene: SCN5A HGNC NCBI

ClinVar Allele:

909560

ClinVar RCV:

RCV001841009

ClinVar Variation:

925641

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Pro564Ser	CA352146692 NM_000335.5:c.1690C>T