Allele Registry

Canonical Allele Identifier: PA645501748

Gene: WDR19 HGNC NCBI

ClinVar Allele:

270914

ClinVar RCV:

RCV000274698

RCV001088018

RCV002519251

ClinVar Variation:

286677

HGVS (amino-acid)	Matching Registered Transcripts
NP_079408.3:p.Gly789Ser	CA2892066 NM_025132.4:c.2365G>A