Canonical Allele Identifier: PA2825161431
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2198355
ClinVar RCV Id: RCV002629325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr346Lys
CA379960307
NM_000378.6:c.1037C>A