Canonical Allele Identifier: PA2829998802
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2950348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gln31Glu
CA219511455
NM_024424.5:c.91C>G