Allele Registry

Canonical Allele Identifier: PA265045

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058487

RCV003539779

ClinVar Variation:

67720

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Ala735Glu	CA015938 NM_001099404.2:c.2204C>A