Canonical Allele Identifier: PA2826222867
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388957
ClinVar RCV Id: RCV001886927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Thr146Arg
CA379960306
NM_001198551.1:c.437C>G