Canonical Allele Identifier: PA2829998686
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2012914
ClinVar RCV Id: RCV002843467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr12Lys
CA379966526
NM_024424.5:c.35C>A