Canonical Allele Identifier: PA2830000529
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg467Pro
CA016330
NM_024424.5:c.1400G>C