Canonical Allele Identifier: PA162823
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135455
ClinVar RCV Id: RCV000122313 RCV000231832 RCV001107196 RCV001107195 RCV001107197 RCV003460864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Arg168Gln
CA016505
NM_001198551.1:c.503G>A