Canonical Allele Identifier: PA2825161328
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496157
ClinVar RCV Id: RCV002028443 RCV004011094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Met302Lys
CA379962185
NM_000378.6:c.905T>A