Canonical Allele Identifier: PA2826972744
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 900898
ClinVar RCV Id: RCV001146433 RCV001146434
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Asp650Glu
CA356637255
NM_001317924.2:c.1950T>A
CA356637256
NM_001317924.2:c.1950T>G