Canonical Allele Identifier: PA2828515817
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361367.1:p.Tyr586Cys
CA8957903
NM_001374438.1:c.1757A>G