Canonical Allele Identifier: PA2741986818
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945688
ClinVar RCV Id: RCV003803782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala128Glu
CA379965806
NM_024426.6:c.383C>A