Canonical Allele Identifier: PA2742016029
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606799
ClinVar RCV Id: RCV003354950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689561.2:p.Asp134Glu
CA286873986
NM_152348.4:c.402C>G
CA397594709
NM_152348.4:c.402C>A