Canonical Allele Identifier: PA2829998652
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948393
ClinVar RCV Id: RCV003807215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Asp8Val
CA379966546
NM_024424.5:c.23A>T