Allele Registry

Canonical Allele Identifier: PA2825160908

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 1474261

ClinVar RCV Id: RCV001971136

ClinVar Variation Id: 2937658

ClinVar RCV Id: RCV003794288

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Ser163Arg	CA379964901 NM_000378.6:c.489C>G CA379964903 NM_000378.6:c.489C>A CA379964913 NM_000378.6:c.487A>C