Canonical Allele Identifier: PA2827718417
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340141.1:p.Tyr702Cys
CA8957903
NM_001353212.3:c.2105A>G