Canonical Allele Identifier: PA2827718378
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2105523
ClinVar RCV Id: RCV003023493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340141.1:p.Tyr575Phe
CA402508928
NM_001353212.3:c.1724A>T