Canonical Allele Identifier: PA2829999456
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 807722
ClinVar RCV Id: RCV000995915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly175Cys
CA379964782
NM_024424.5:c.523G>T