Canonical Allele Identifier: PA2828276066
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476690
ClinVar RCV Id: RCV000538982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.His112Gln
CA379957558
NM_001367854.1:c.336C>A
CA379957559
NM_001367854.1:c.336C>G