Canonical Allele Identifier: PA2580461112
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188226
ClinVar RCV Id: RCV002620071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Val38Ile
CA379966358
NM_024426.6:c.112G>A