Allele Registry

Canonical Allele Identifier: PA218880

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058536

RCV001842320

ClinVar Variation:

67766

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Arg971Cys	CA016616 NM_001099404.2:c.2911C>T