Allele Registry

Canonical Allele Identifier: PA307979

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000183166

RCV000208172

RCV000240624

RCV001836637

RCV001842934

RCV002336464

RCV002500545

RCV003322601

ClinVar Variation:

201572

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Phe1616del	CA018642 NM_000335.5:c.4847_4849del