Allele Registry

Canonical Allele Identifier: PA2825128335

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003539999

ClinVar Variation:

532111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Val95Leu	CA060971 NM_000335.5:c.283G>C CA352157105 NM_000335.5:c.283G>T