Canonical Allele Identifier: PA116270
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3491
ClinVar RCV Id: RCV000003663 RCV004547456
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Arg250Pro
CA016330
NM_001198551.1:c.749G>C