Allele Registry

Canonical Allele Identifier: PA2826972814

Gene: WDR19 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

177355

ClinVar RCV:

RCV000154140

RCV000278329

RCV000317115

RCV000723861

RCV001083264

RCV002277304

RCV002516102

RCV004532742

ClinVar Variation:

167843

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304853.1:p.Tyr771Ser	CA235263 NM_001317924.2:c.2312A>C