Allele Registry

Canonical Allele Identifier: PA265837

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058772

ClinVar Variation:

67986

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Ala178Gly	CA019140 NM_000335.5:c.533C>G