Allele Registry

Canonical Allele Identifier: PA658809195

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003539999

ClinVar Variation:

532111

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Val95Leu	CA060971 NM_198056.3:c.283G>C CA352157105 NM_198056.3:c.283G>T