Canonical Allele Identifier: PA2826224404
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Arg233Gln
CA16619314
NM_001198552.2:c.698G>A