Canonical Allele Identifier: PA2826223589
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543128
ClinVar RCV Id: RCV000653791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Met290Val
CA379957543
NM_001198551.1:c.868A>G