Allele Registry

Canonical Allele Identifier: PA2829955718

Gene: WDR35 HGNC NCBI

ClinVar Variation Id: 440416

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Lys1112Arg	CA1542695 NM_020779.4:c.3335A>G