Canonical Allele Identifier: PA2826224335
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Cys199Gly
CA016265
NM_001198552.2:c.595T>G