Allele Registry

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Canonical Allele Identifier: PA2829999414

Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474261

ClinVar RCV Id: RCV001971136

ClinVar Variation Id: 2937658

ClinVar RCV Id: RCV003794288

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Ser163Arg	CA379964901 NM_024424.5:c.489C>G CA379964903 NM_024424.5:c.489C>A CA379964913 NM_024424.5:c.487A>C