Allele Registry

Canonical Allele Identifier: PA2825940375

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058866

ClinVar Variation:

68062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Leu325Arg	CA019964 NM_001160160.2:c.974T>G