Canonical Allele Identifier: PA2825160569
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241478
ClinVar RCV Id: RCV000229513 RCV001105881 RCV001104737 RCV001105882 RCV001563568 RCV001820764 RCV002257598 RCV002519803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly65Arg
CA064714
NM_000378.6:c.193G>A
CA379966189
NM_000378.6:c.193G>C