Canonical Allele Identifier: PA254760
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Tyr1795Cys
CA019196
NM_001099404.2:c.5384A>G