Canonical Allele Identifier: PA2826224367
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3495
ClinVar RCV Id: RCV000003667 RCV000003668 RCV002512715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.His216Tyr
CA016298
NM_001198552.2:c.646C>T