Canonical Allele Identifier: PA916075366
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 642281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala66Thr
CA379966185
NM_024426.6:c.196G>A