Canonical Allele Identifier: PA2825497102
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Tyr1777Cys
CA019196
NM_001099405.2:c.5330A>G