Canonical Allele Identifier: PA2828516004
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361368.1:p.Tyr585Cys
CA8957903
NM_001374439.1:c.1754A>G