Canonical Allele Identifier: PA2825160810
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449277
ClinVar RCV Id: RCV002014474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro134Arg
CA379965776
NM_000378.6:c.401C>G