Canonical Allele Identifier: PA2829999404
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 934034
ClinVar RCV Id: RCV001202363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gln160Glu
CA379964946
NM_024424.5:c.478C>G