Canonical Allele Identifier: PA2829999400
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383500
ClinVar RCV Id: RCV001892642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Glu159Asp
CA379964949
NM_024424.5:c.477G>T
CA379964951
NM_024424.5:c.477G>C