Canonical Allele Identifier: PA2825160834
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2953840
ClinVar RCV Id: RCV003813063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro141Leu
CA379965699
NM_000378.6:c.422C>T