Canonical Allele Identifier: PA2829999180
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly117Asp
CA219511109
NM_024424.5:c.350G>A