Canonical Allele Identifier: PA2829999435
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Val167Ile
CA379964871
NM_024424.5:c.499G>A