Allele Registry

Canonical Allele Identifier: PA2829955703

Gene: WDR35 HGNC NCBI

ClinVar Variation Id: 440412

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Tyr1057Cys	CA1542728 NM_020779.4:c.3170A>G