Canonical Allele Identifier: PA2827719175
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_001340145.1:p.Tyr521Phe
CA402508928
NM_001353216.3:c.1562A>T