Canonical Allele Identifier: PA2830000148
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2198355
ClinVar RCV Id: RCV002629325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr363Lys
CA379960307
NM_024424.5:c.1088C>A