Canonical Allele Identifier: PA2829998826
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188226
ClinVar RCV Id: RCV002620071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Val38Ile
CA379966358
NM_024424.5:c.112G>A