Canonical Allele Identifier: PA891863834
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304423
ClinVar RCV Id: RCV000354093 RCV000397632 RCV000653778 RCV003324741 RCV000313309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly196Asp
CA065067
NM_024426.6:c.587G>A