Canonical Allele Identifier: PA2573283096
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484902
ClinVar RCV Id: RCV002030271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ile361Thr
CA379960334
NM_024426.6:c.1082T>C