Allele Registry

Canonical Allele Identifier: PA107793

Gene: SCN5A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

24416

ClinVar RCV:

RCV000009972

RCV000009973

RCV000009974

RCV000058773

RCV000183117

RCV000208193

RCV000245905

RCV000588022

RCV000824758

RCV003591625

RCV004545722

ClinVar Variation:

9377

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Glu1784Lys	CA019148 NM_198056.3:c.5350G>A