Canonical Allele Identifier: PA2828515259
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 326889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361364.1:p.Val591Met
CA8957911
NM_001374435.1:c.1771G>A