Canonical Allele Identifier: PA891863780
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Trp45Arg
CA379966318
NM_024426.6:c.133T>C
CA379966319
NM_024426.6:c.133T>A