Canonical Allele Identifier: PA2826972814
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 167843
ClinVar RCV Id: RCV000154140 RCV000317115 RCV000278329 RCV000723861 RCV001083264 RCV002277304 RCV002516102 RCV004532742
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Amino-acid Alleles

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