Canonical Allele Identifier: PA1139690376
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 982855
ClinVar RCV Id: RCV001262568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157281.1:p.Pro161Leu
CA8272983
NM_001163809.2:c.482C>T