Canonical Allele Identifier: PA2825160898
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 934034
ClinVar RCV Id: RCV001202363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gln160Glu
CA379964946
NM_000378.6:c.478C>G