Canonical Allele Identifier: PA116258
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3488
ClinVar RCV Id: RCV000003659 RCV000484493 RCV001250546 RCV002243617 RCV001851622 RCV002496247 RCV003147274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Arg222His
CA016285
NM_001198551.1:c.665G>A