Canonical Allele Identifier: PA162815
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.His147Gln
CA016478
NM_001198551.1:c.441C>A
CA379960289
NM_001198551.1:c.441C>G