Allele Registry

Canonical Allele Identifier: PA145064

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058402

ClinVar Variation:

67645

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Gly400Ala	CA014496 NM_000335.5:c.1199G>C