Canonical Allele Identifier: PA2825963183
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 3190272
ClinVar RCV Id: RCV004480698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157281.1:p.Ser1094Ala
CA397593567
NM_001163809.2:c.3280T>G