Canonical Allele Identifier: PA2829999438
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Val167Ala
CA379964865
NM_024424.5:c.500T>C