Canonical Allele Identifier: PA2825160790
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719758
ClinVar RCV Id: RCV002303952 RCV003464439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro131Thr
CA219511089
NM_000378.6:c.391C>A