Canonical Allele Identifier: PA2829998842
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg39Pro
CA379966350
NM_024424.5:c.116G>C