Allele Registry

Canonical Allele Identifier: PA2827922281

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003772435

ClinVar Variation:

1349790

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Pro773Thr	CA352143439 NM_001354701.2:c.2317C>A