Canonical Allele Identifier: PA2829999332
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074353
ClinVar RCV Id: RCV004012895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Lys146Gln
CA379965638
NM_024424.5:c.436A>C