Canonical Allele Identifier: PA2829999455
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 939598
ClinVar RCV Id: RCV001209022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly175Asp
CA379964781
NM_024424.5:c.524G>A