Canonical Allele Identifier: PA2825160424
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099628
ClinVar RCV Id: RCV003021810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg24Pro
CA379966446
NM_000378.6:c.71G>C