Allele Registry

Canonical Allele Identifier: PA265839

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058772

ClinVar Variation:

67986

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Ala178Gly	CA019140 NM_198056.3:c.533C>G