Canonical Allele Identifier: PA2826972893
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 127158
ClinVar RCV Id: RCV000115014 RCV000433622 RCV000754960 RCV000653250 RCV000850617 RCV001262101 RCV003224149 RCV003224150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Arg1018Gln
CA151412
NM_001317924.2:c.3053G>A