Allele Registry

Canonical Allele Identifier: PA236809

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000171697

RCV000855502

RCV001842522

ClinVar Variation:

191499

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Ser1738Phe	CA018989 NM_198056.3:c.5213C>T