Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434815G>ACA473571428WT1c.546C>T (p.Tyr182=)
c.531C>T (p.Tyr177=)
n.725C>T
 ClinVar dbSNP gnomAD v4
11g.32434815G>TCA016351WT1c.546C>A (p.Tyr182Ter)
c.531C>A (p.Tyr177Ter)
n.725C>A
 ClinVar dbSNP

Number of alleles fetched