Canonical Allele Identifier: PA2825160750
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018324
ClinVar RCV Id: RCV001317608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser119Trp
CA379965861
NM_000378.6:c.356C>G