Canonical Allele Identifier: PA916047002
Gene: WT1 HGNC NCBI
ClinVar RCV:
RCV000003664
ClinVar Variation:
3492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Cys7Tyr
CA016258
NM_001367854.1:c.20G>A