Allele Registry

Canonical Allele Identifier: PA2825492315

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058772

ClinVar Variation:

67986

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092875.1:p.Ala178Gly	CA019140 NM_001099405.2:c.533C>G