Canonical Allele Identifier: PA2829999452
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437098
ClinVar RCV Id: RCV001946529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr174Ala
CA379964793
NM_024424.5:c.520A>G