Allele Registry

Canonical Allele Identifier: PA1139758695

Gene: SCN5A HGNC NCBI

ClinVar Allele:

909560

ClinVar RCV:

RCV001841009

ClinVar Variation:

925641

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Pro564Ser	CA352146692 NM_198056.3:c.1690C>T