Canonical Allele Identifier: PA2829998902
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304429
ClinVar Variation Id: 1426420
ClinVar RCV Id: RCV001931279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser54Arg
CA064646
NM_024424.5:c.162C>G
CA379966253
NM_024424.5:c.162C>A
CA379966259
NM_024424.5:c.160A>C