Canonical Allele Identifier: PA2580234026
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361357.1:p.Tyr703Cys
CA8957903
NM_001374428.1:c.2108A>G