Canonical Allele Identifier: PA2826222880
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2923287
ClinVar RCV Id: RCV003780405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Gly148Arg
CA379960286
NM_001198551.1:c.442G>C