Canonical Allele Identifier: PA2829998800
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Cys29Tyr
CA219511456
NM_024424.5:c.86G>A