Allele Registry

Canonical Allele Identifier: PA2826972728

Gene: WDR19 HGNC NCBI

ClinVar RCV:

RCV000274698

RCV001088018

RCV002519251

ClinVar Variation:

286677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304853.1:p.Gly629Ser	CA2892066 NM_001317924.2:c.1885G>A