Canonical Allele Identifier: PA2825160573
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 642281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala66Thr
CA379966185
NM_000378.6:c.196G>A