Canonical Allele Identifier: PA2829999429
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474384
ClinVar RCV Id: RCV002005490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala164Pro
CA379964899
NM_024424.5:c.490G>C