Canonical Allele Identifier: PA2828516574
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361372.1:p.Tyr457Cys
CA8957903
NM_001374443.1:c.1370A>G