Canonical Allele Identifier: PA2573283097
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388957
ClinVar RCV Id: RCV001886927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Thr363Arg
CA379960306
NM_024426.6:c.1088C>G