Canonical Allele Identifier: PA2829999233
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 658496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro127Arg
CA379965811
NM_024424.5:c.380C>G