Canonical Allele Identifier: PA2826224074
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3499
ClinVar RCV Id: RCV000003673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Ser112Gly
CA016356
NM_001198552.2:c.334A>G