Canonical Allele Identifier: PA2825160751
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 651615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala120Thr
CA379965859
NM_000378.6:c.358G>A