Canonical Allele Identifier: PA2825538033
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.His558Cys
CA1139655765
NM_001099404.2:c.1672_1673delinsTG