Canonical Allele Identifier: PA2829998952
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser63Arg
CA379966197
NM_024424.5:c.189C>G
CA379966198
NM_024424.5:c.189C>A
CA379966202
NM_024424.5:c.187A>C