Canonical Allele Identifier: PA116290
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3498
ClinVar RCV Id: RCV000003672
ClinVar Variation Id: 973193
ClinVar RCV Id: RCV001280531 RCV001879755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.His229Gln
CA016292
NM_001198551.1:c.687C>G
CA379959168
NM_001198551.1:c.687C>A