Canonical Allele Identifier: PA2829999186
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543139
ClinVar RCV Id: RCV000653802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser119Pro
CA379965864
NM_024424.5:c.355T>C