Canonical Allele Identifier: PA2825160527
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Glu52Lys
CA379966273
NM_000378.6:c.154G>A