Canonical Allele Identifier: PA1139759141
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_079408.3:p.Asp810Glu
CA356637255
NM_025132.4:c.2430T>A
CA356637256
NM_025132.4:c.2430T>G