Canonical Allele Identifier: PA2825160674
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 843222
ClinVar RCV Id: RCV001045790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Leu99Gln
CA379965983
NM_000378.6:c.296T>A