Canonical Allele Identifier: PA2825161634
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137049
ClinVar RCV Id: RCV003062358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Cys441Arg
CA379958962
NM_000378.6:c.1321T>C