Canonical Allele Identifier: PA2741986906
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2923287
ClinVar RCV Id: RCV003780405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly365Arg
CA379960286
NM_024426.6:c.1093G>C