Canonical Allele Identifier: PA2825160379
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522020
ClinVar RCV Id: RCV002034216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr12Met
CA379966524
NM_000378.6:c.35C>T