Allele Registry

Canonical Allele Identifier: PA2825945312

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058715

RCV000144031

RCV001836727

RCV001842371

RCV002477202

ClinVar Variation:

67932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153633.1:p.Thr1566Met	CA018653 NM_001160161.2:c.4697C>T CA085295 NM_001160161.2:c.[4697C>T;3532C>T]