Canonical Allele Identifier: PA2826972891
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 988209
ClinVar RCV Id: RCV001328231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Leu1016Phe
CA356647364
NM_001317924.2:c.3046C>T