Canonical Allele Identifier: PA2829998940
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1375792
ClinVar RCV Id: RCV001902527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gln59Arg
CA379966225
NM_024424.5:c.176A>G