Canonical Allele Identifier: PA2829999147
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 654983
ClinVar RCV Id: RCV000811058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala114Glu
CA379965886
NM_024424.5:c.341C>A