Canonical Allele Identifier: PA2825160952
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 951827
ClinVar RCV Id: RCV001223822 RCV003462762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg181Pro
CA379964720
NM_000378.6:c.542G>C