Canonical Allele Identifier: PA916022106
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 424472
ClinVar RCV Id: RCV000479045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Leu46Pro
CA16618044
NM_001317924.2:c.137T>C