Canonical Allele Identifier: PA2825161726
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476691
ClinVar RCV Id: RCV000556002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg493Thr
CA379957502
NM_000378.6:c.1478G>C