Canonical Allele Identifier: PA2826224049
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 847109
ClinVar RCV Id: RCV001050583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Thr102Asn
CA219496195
NM_001198552.2:c.305C>A