Canonical Allele Identifier: PA2829998920
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 933960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg57Leu
CA219511348
NM_024424.5:c.170G>T