Canonical Allele Identifier: PA916047017
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Arg71Pro
CA016330
NM_001367854.1:c.212G>C