Allele Registry

Canonical Allele Identifier: PA2827921438

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058772

ClinVar Variation:

67986

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Ala178Gly	CA019140 NM_001354701.2:c.533C>G