Canonical Allele Identifier: PA2825941981
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1738212
ClinVar RCV Id: RCV002333191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Gln1382Pro
CA352146708
NM_001160160.2:c.4145A>C