Canonical Allele Identifier: PA2830298415
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 3190272
ClinVar RCV Id: RCV004480698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689561.2:p.Ser43Ala
CA397593567
NM_152348.4:c.127T>G