Canonical Allele Identifier: PA2829999407
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930097
ClinVar RCV Id: RCV003787455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Cys161Gly
CA379964931
NM_024424.5:c.481T>G