Canonical Allele Identifier: PA2829998963
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala66Glu
CA379966182
NM_024424.5:c.197C>A