Canonical Allele Identifier: PA2828515076
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361363.1:p.Tyr610Cys
CA8957903
NM_001374434.1:c.1829A>G