Canonical Allele Identifier: PA916075421
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 651615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala120Thr
CA379965859
NM_024426.6:c.358G>A