Canonical Allele Identifier: PA2826222637
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2924237
ClinVar RCV Id: RCV003785987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Cys91Tyr
CA379962145
NM_001198551.1:c.272G>A