Canonical Allele Identifier: PA2829998765
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 839396
ClinVar RCV Id: RCV001041139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg24His
CA379966447
NM_024424.5:c.71G>A