Canonical Allele Identifier: PA2829999023
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 715223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala87Thr
CA064789
NM_024424.5:c.259G>A