Canonical Allele Identifier: PA2829999272
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490734
ClinVar RCV Id: RCV001983890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro134Ser
CA379965777
NM_024424.5:c.400C>T