Canonical Allele Identifier: PA2828516441
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 3086422
ClinVar RCV Id: RCV004379816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361371.1:p.Tyr452Cys
CA8957907
NM_001374442.1:c.1355A>G