Canonical Allele Identifier: PA2825538788
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Cys1176Arg
CA352138278
NM_001099404.2:c.3526T>C