Canonical Allele Identifier: PA2825963190
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 2210572
ClinVar RCV Id: RCV002664696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157281.1:p.Ser1184Phe
CA8273277
NM_001163809.2:c.3551C>T