Canonical Allele Identifier: PA2829999323
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 944633
ClinVar RCV Id: RCV001215074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser143Pro
CA379965677
NM_024424.5:c.427T>C