Canonical Allele Identifier: PA2829999471
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2940962
ClinVar RCV Id: RCV003792224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Cys180Tyr
CA379964735
NM_024424.5:c.539G>A