Allele Registry

Canonical Allele Identifier: PA265943

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058850

RCV000182949

RCV000240636

RCV000781844

RCV003996556

ClinVar Variation:

68047

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Arg282Cys	CA019844 NM_000335.5:c.844C>T