Canonical Allele Identifier: PA891863876
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419332
ClinVar RCV Id: RCV000484903 RCV002294337 RCV003766670 RCV002506163 RCV003458440 RCV004551581 RCV003147478 RCV003225075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg467Gln
CA16619314
NM_024426.6:c.1400G>A