Allele Registry

Canonical Allele Identifier: PA658678210

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003654421

ClinVar Variation:

463304

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Asn598Ser	CA352146132 NM_198056.3:c.1793A>G