Canonical Allele Identifier: PA2825944944
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1738212
ClinVar RCV Id: RCV002333191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gln1329Pro
CA352146708
NM_001160161.2:c.3986A>C