Canonical Allele Identifier: PA2825128239
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 920699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala60Pro
CA352158329
NM_000335.5:c.178G>C