Canonical Allele Identifier: PA891863784
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_077744.4:p.Ser54Arg
CA064646
NM_024426.6:c.162C>G
CA379966253
NM_024426.6:c.162C>A
CA379966259
NM_024426.6:c.160A>C