Canonical Allele Identifier: PA2825161423
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484902
ClinVar RCV Id: RCV002030271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ile344Thr
CA379960334
NM_000378.6:c.1031T>C