Allele Registry

Canonical Allele Identifier: PA265712

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058721

RCV000489058

RCV000709763

ClinVar Variation:

67937

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Arg1629Gln	CA018714 NM_001099404.2:c.4886G>A