Canonical Allele Identifier: PA2826972929
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 127157
ClinVar RCV Id: RCV000115013 RCV000788500 RCV001281118 RCV001854544 RCV002477273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Glu1075Lys
CA151410
NM_001317924.2:c.3223G>A