Canonical Allele Identifier: PA2828515263
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361364.1:p.Tyr609Cys
CA8957903
NM_001374435.1:c.1826A>G