Canonical Allele Identifier: PA2829998960
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 646844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly65Trp
CA379966190
NM_024424.5:c.193G>T