Canonical Allele Identifier: PA2829998939
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1518459
ClinVar RCV Id: RCV002021760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gln59His
CA379966222
NM_024424.5:c.177G>T
CA379966223
NM_024424.5:c.177G>C