Allele Registry

Canonical Allele Identifier: PA916050546

Gene: WDR35 HGNC NCBI

ClinVar Allele:

488635

ClinVar RCV:

RCV000592980

RCV001139418

RCV001139419

RCV001370744

RCV004543315

ClinVar Variation:

497211

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Pro351Ala	CA1543357 NM_020779.4:c.1051C>G