Canonical Allele Identifier: PA916022120
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 440411
ClinVar RCV Id: RCV001227801 RCV001811019 RCV002481645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Arg943Gln
CA2892335
NM_001317924.2:c.2828G>A