Canonical Allele Identifier: PA2826972458
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514580
ClinVar RCV Id: RCV002029401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Ala111Val
CA95686331
NM_001317924.2:c.332C>T