Canonical Allele Identifier: PA2826222644
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2151387
ClinVar RCV Id: RCV003061316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Thr93Pro
CA379962129
NM_001198551.1:c.277A>C