Canonical Allele Identifier: PA2827717967
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_001340139.1:p.Tyr520Phe
CA402508928
NM_001353210.3:c.1559A>T