Canonical Allele Identifier: PA2825160550
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1375792
ClinVar RCV Id: RCV001902527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gln59Arg
CA379966225
NM_000378.6:c.176A>G