Allele Registry

Canonical Allele Identifier: PA2825945630

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010005

RCV000058782

RCV000171695

RCV000183199

RCV000987198

RCV001507624

RCV001841243

RCV001842769

RCV002345238

RCV002491518

RCV003163406

ClinVar Variation:

9402

920535

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153633.1:p.Asp1765Asn	CA019238 NM_001160161.2:c.5293G>A CA913188086 NM_001160161.2:c.5293_5295delinsAAC