Canonical Allele Identifier: PA2825538189
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 921748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg693His
CA059728
NM_001099404.2:c.2078G>A