Canonical Allele Identifier: PA2829998637
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2155557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Leu6Gly
CA2580084217
NM_024424.5:c.16_17delinsGG