Canonical Allele Identifier: PA2825161432
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388957
ClinVar RCV Id: RCV001886927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr346Arg
CA379960306
NM_000378.6:c.1037C>G