Canonical Allele Identifier: PA2825160442
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543133
ClinVar RCV Id: RCV000653796 RCV004004101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Cys29Tyr
CA219511456
NM_000378.6:c.86G>A