Canonical Allele Identifier: PA2828514861
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_001361362.1:p.Tyr521Phe
CA402508928
NM_001374433.1:c.1562A>T