Allele Registry

Canonical Allele Identifier: PA916050509

Gene: WDR35 HGNC NCBI

ClinVar Variation Id: 431796

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Gly69Asp	CA43388469 NM_020779.4:c.206G>A