Allele Registry

Canonical Allele Identifier: PA264882

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058391

RCV004017376

ClinVar Variation:

67634

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Arg367Leu	CA014324 NM_001099404.2:c.1100G>T