Canonical Allele Identifier: PA2825160847
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074353
ClinVar RCV Id: RCV004012895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Lys146Gln
CA379965638
NM_000378.6:c.436A>C