Allele Registry

Canonical Allele Identifier: PA093055

Gene: WDR19 HGNC NCBI

ClinVar RCV:

RCV000023684

ClinVar Variation:

30706

HGVS (amino-acid)	Matching Registered Transcripts
NP_079408.3:p.Val345Gly	CA129408 NM_025132.4:c.1034T>G