Canonical Allele Identifier: PA916047015
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Arg71Gln
CA16619314
NM_001367854.1:c.212G>A