Canonical Allele Identifier: PA891863792
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476696
ClinVar RCV Id: RCV000544002 RCV001591301 RCV002256394 RCV002491099 RCV002527933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gln73Leu
CA219511297
NM_024426.6:c.218A>T