Canonical Allele Identifier: PA2829998792
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072554
ClinVar RCV Id: RCV004013576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro27Ser
CA379966432
NM_024424.5:c.79C>T