Canonical Allele Identifier: PA2826972460
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374474
ClinVar RCV Id: RCV001883110 RCV002482598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Arg112Cys
CA2891709
NM_001317924.2:c.334C>T