Allele Registry

Canonical Allele Identifier: PA645501748

Gene: WDR19 HGNC NCBI

ClinVar Variation Id: 286677

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