Allele Registry

Canonical Allele Identifier: PA2825129919

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003772435

ClinVar Variation:

1349790

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Pro773Thr	CA352143439 NM_000335.5:c.2317C>A