Canonical Allele Identifier: PA2829999291
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 836130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro137Ala
CA379965745
NM_024424.5:c.409C>G