Canonical Allele Identifier: PA2825160378
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2012914
ClinVar RCV Id: RCV002843467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr12Lys
CA379966526
NM_000378.6:c.35C>A