Canonical Allele Identifier: PA891863791
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241479
ClinVar RCV Id: RCV000232293 RCV000239344 RCV000390844 RCV000347621 RCV001697685 RCV001820765 RCV002243921 RCV002243920 RCV004547615
ClinVar Variation Id: 1018609
ClinVar RCV Id: RCV001317936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gln72His
CA064754
NM_024426.6:c.216G>T
CA379966142
NM_024426.6:c.216G>C