Allele Registry

Canonical Allele Identifier: PA913199158

Gene: WDR35 HGNC NCBI

ClinVar RCV:

RCV000754964

RCV002531368

ClinVar Variation:

558762

HGVS (amino-acid)	Matching Registered Transcripts
NP_001006658.1:p.Glu1149Lys	CA43853337 NM_001006657.2:c.3445G>A