Canonical Allele Identifier: PA2825491981
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 920699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala60Pro
CA352158329
NM_001099405.2:c.178G>C