Allele Registry

Canonical Allele Identifier: PA145066

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058402

ClinVar Variation:

67645

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Gly400Ala	CA014496 NM_198056.3:c.1199G>C