Canonical Allele Identifier: PA2826222656
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 620630
ClinVar RCV Id: RCV000761158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Gly100Glu
CA379962044
NM_001198551.1:c.299G>A