Canonical Allele Identifier: PA2827718821
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 3086422
ClinVar RCV Id: RCV004379816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340143.1:p.Tyr697Cys
CA8957907
NM_001353214.3:c.2090A>G