Canonical Allele Identifier: PA2829999234
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476701
ClinVar RCV Id: RCV000533914
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro127Thr
CA379965815
NM_024424.5:c.379C>A