Canonical Allele Identifier: PA2830001898
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476712
ClinVar RCV Id: RCV000524589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Thr224Ser
CA379963596
NM_024426.6:c.670A>T