Canonical Allele Identifier: PA2829999300
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 848604
ClinVar RCV Id: RCV001052395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro138Arg
CA379965734
NM_024424.5:c.413C>G