Canonical Allele Identifier: PA891863768
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 569272
ClinVar RCV Id: RCV000689861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro9Arg
CA379966539
NM_024426.6:c.26C>G