Canonical Allele Identifier: PA2830000130
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484902
ClinVar RCV Id: RCV002030271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ile361Thr
CA379960334
NM_024424.5:c.1082T>C