Canonical Allele Identifier: PA186047
Gene: WDR93 HGNC NCBI

Linked Data

ClinVar Variation Id: 183287
ClinVar RCV Id: RCV000162108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064597.1:p.Tyr94His
CA186046
NM_020212.2:c.280T>C