Canonical Allele Identifier: PA2829999238
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945688
ClinVar RCV Id: RCV003803782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala128Glu
CA379965806
NM_024424.5:c.383C>A