Canonical Allele Identifier: PA916047004
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Arg43His
CA016285
NM_001367854.1:c.128G>A