Canonical Allele Identifier: PA891863803
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 570963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro115His
CA379965883
NM_024426.6:c.344C>A