Canonical Allele Identifier: PA2829999750
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Met255Lys
CA016452
NM_024424.5:c.764T>A