Canonical Allele Identifier: PA2825160877
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1476011
ClinVar RCV Id: RCV001977729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro156Gln
CA379964991
NM_000378.6:c.467C>A