Canonical Allele Identifier: PA2825160722
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2942720
ClinVar RCV Id: RCV003807886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Phe113Tyr
CA379965896
NM_000378.6:c.338T>A