Canonical Allele Identifier: PA2828516175
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2078682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361369.1:p.Tyr572Cys
CA8957903
NM_001374440.1:c.1715A>G