Allele Registry

Canonical Allele Identifier: PA2825128785

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003539997

ClinVar Variation:

532098

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Arg282Gly	CA352150552 NM_000335.5:c.844C>G