Canonical Allele Identifier: PA2829999446
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly171Val
CA379964820
NM_024424.5:c.512G>T