Canonical Allele Identifier: PA2826224122
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.His130Gln
CA016478
NM_001198552.2:c.390C>A
CA379960289
NM_001198552.2:c.390C>G