Canonical Allele Identifier: PA2829998958
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027021
ClinVar RCV Id: RCV001327560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly65Glu
CA379966188
NM_024424.5:c.194G>A