Allele Registry

Canonical Allele Identifier: PA2827921617

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058866

ClinVar Variation:

68062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Leu325Arg	CA019964 NM_001354701.2:c.974T>G