Canonical Allele Identifier: PA2826224491
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476690
ClinVar RCV Id: RCV000538982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.His274Gln
CA379957558
NM_001198552.2:c.822C>A
CA379957559
NM_001198552.2:c.822C>G