Allele Registry

Canonical Allele Identifier: PA2825537700

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003539997

ClinVar Variation:

532098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Arg282Gly	CA352150552 NM_001099404.2:c.844C>G