Canonical Allele Identifier: PA093055
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 30706
ClinVar RCV Id: RCV000023684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Val345Gly
CA129408
NM_025132.4:c.1034T>G