Canonical Allele Identifier: PA2825130889
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Cys1175Arg
CA352138278
NM_000335.5:c.3523T>C