Canonical Allele Identifier: PA2825161592
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3496
ClinVar RCV Id: RCV000003669 RCV002512716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Cys416Gly
CA016265
NM_000378.6:c.1246T>G