Canonical Allele Identifier: PA2829999696
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly234Arg
CA379963498
NM_024424.5:c.700G>C