Canonical Allele Identifier: PA2828276014
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Cys37Gly
CA016265
NM_001367854.1:c.109T>G