Allele Registry

Canonical Allele Identifier: PA2827921312

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003539999

ClinVar Variation:

532111

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Val95Leu	CA060971 NM_001354701.2:c.283G>C CA352157105 NM_001354701.2:c.283G>T