Canonical Allele Identifier: PA162819
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41847
ClinVar RCV Id: RCV000034780 RCV000122312 RCV000709139 RCV001081983 RCV002255123 RCV004549406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Cys138Arg
CA016364
NM_001198551.1:c.412T>C