Canonical Allele Identifier: PA2829999169
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2932914
ClinVar RCV Id: RCV003798080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro116Arg
CA379965877
NM_024424.5:c.347C>G