Canonical Allele Identifier: PA2829998766
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099628
ClinVar RCV Id: RCV003021810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg24Pro
CA379966446
NM_024424.5:c.71G>C