Canonical Allele Identifier: PA2829999907
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Met302Lys
CA379962185
NM_024424.5:c.905T>A