Canonical Allele Identifier: PA2825160553
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1999647
ClinVar RCV Id: RCV002819753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg61Trp
CA379966215
NM_000378.6:c.181C>T