Canonical Allele Identifier: PA2826972728
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 286677
ClinVar RCV Id: RCV000274698 RCV002519251 RCV001088018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Gly629Ser
CA2892066
NM_001317924.2:c.1885G>A