Allele Registry

Canonical Allele Identifier: PA2825943119

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003539999

ClinVar Variation:

532111

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153633.1:p.Val95Leu	CA060971 NM_001160161.2:c.283G>C CA352157105 NM_001160161.2:c.283G>T