Canonical Allele Identifier: PA2829998674
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057387
ClinVar RCV Id: RCV001366357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser11Cys
CA379966529
NM_024424.5:c.32C>G