Canonical Allele Identifier: PA2829998653
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 849084
ClinVar RCV Id: RCV001052969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro9Thr
CA379966543
NM_024424.5:c.25C>A