Canonical Allele Identifier: PA2828516309
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361370.1:p.Tyr513Cys
CA8957903
NM_001374441.1:c.1538A>G