Canonical Allele Identifier: PA2826222369
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476716
ClinVar RCV Id: RCV000543084 RCV003459258 RCV003999466 RCV003228953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Gly17Arg
CA379963498
NM_001198551.1:c.49G>C