Canonical Allele Identifier: PA186049
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 183290
ClinVar RCV Id: RCV000162111 RCV000171248 RCV000660890 RCV003987381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157281.1:p.Gly282Glu
CA186048
NM_001163809.2:c.845G>A