Canonical Allele Identifier: PA891863783
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly49Val
CA379966285
NM_024426.6:c.146G>T