Canonical Allele Identifier: PA1139750473
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 951827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg181Pro
CA379964720
NM_024426.6:c.542G>C