Allele Registry

Canonical Allele Identifier: PA2825941039

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003772435

ClinVar Variation:

1349790

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Pro773Thr	CA352143439 NM_001160160.2:c.2317C>A