Canonical Allele Identifier: PA2825160536
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1809679
ClinVar RCV Id: RCV002496211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala55Thr
CA379966252
NM_000378.6:c.163G>A