Canonical Allele Identifier: PA116274
Gene: WT1 HGNC NCBI
ClinVar RCV:
RCV000003664
ClinVar Variation:
3492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Cys186Tyr
CA016258
NM_001198551.1:c.557G>A