Canonical Allele Identifier: PA2830002780
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg467Pro
CA016330
NM_024426.6:c.1400G>C