Allele Registry

Canonical Allele Identifier: PA916050551

Gene: WDR35 HGNC NCBI

ClinVar RCV:

RCV000395590

RCV000515966

RCV001086026

RCV001143732

RCV001143733

RCV002278315

ClinVar Variation:

288569

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Asn395Tyr	CA1543330 NM_020779.4:c.1183A>T