Canonical Allele Identifier: PA2580198569
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2068704
ClinVar RCV Id: RCV002975029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Leu51Val
CA356633803
NM_001317924.2:c.151T>G