Canonical Allele Identifier: PA891863776
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Cys29Tyr
CA219511456
NM_024426.6:c.86G>A