Canonical Allele Identifier: PA2829998661
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 652024
ClinVar RCV Id: RCV000807502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala10Val
CA219511534
NM_024424.5:c.29C>T