Canonical Allele Identifier: PA891863786
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly65Arg
CA064714
NM_024426.6:c.193G>A
CA379966189
NM_024426.6:c.193G>C