Canonical Allele Identifier: PA2829999436
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 872897
ClinVar RCV Id: RCV001093599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Val167Asp
CA379964866
NM_024424.5:c.500T>A