Canonical Allele Identifier: PA2829999144
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948439
ClinVar RCV Id: RCV003809213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Phe113Ser
CA379965895
NM_024424.5:c.338T>C