Allele Registry

Canonical Allele Identifier: PA2825940487

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058402

ClinVar Variation:

67645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Gly400Ala	CA014496 NM_001160160.2:c.1199G>C