Canonical Allele Identifier: PA2830002205
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2946974
ClinVar RCV Id: RCV003801164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Met314Arg
CA379962080
NM_024426.6:c.941T>G