Allele Registry

Canonical Allele Identifier: PA2825940791

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003551394

ClinVar Variation:

2718907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Gly599Trp	CA352146122 NM_001160160.2:c.1795G>T