Canonical Allele Identifier: PA2827718789
Gene: DYM HGNC NCBI

Linked Data

ClinVar Variation Id: 2105523
ClinVar RCV Id: RCV003023493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340143.1:p.Tyr576Phe
CA402508928
NM_001353214.3:c.1727A>T