Canonical Allele Identifier: PA101242
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 3193
ClinVar RCV Id: RCV000003344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060123.3:p.Cys542Arg
CA116051
NM_017653.6:c.1624T>C