Allele Registry

Canonical Allele Identifier: PA265843

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058781

RCV004546427

ClinVar Variation:

67991

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Cys182Arg	CA019232 NM_000335.5:c.544T>C