Canonical Allele Identifier: PA116282
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3496
ClinVar RCV Id: RCV000003669 RCV002512716
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Cys216Gly
CA016265
NM_001198551.1:c.646T>G