Canonical Allele Identifier: PA891863790
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584766
ClinVar RCV Id: RCV000988522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser69Thr
CA379966167
NM_024426.6:c.205T>A