Allele Registry

Canonical Allele Identifier: PA2825128660

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV004014682

ClinVar Variation:

3071180

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Arg222Leu	CA352151562 NM_000335.5:c.665G>T