Canonical Allele Identifier: PA2829998721
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro17Leu
CA379966490
NM_024424.5:c.50C>T