Canonical Allele Identifier: PA2829998903
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093007
ClinVar RCV Id: RCV003008350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser54Thr
CA379966255
NM_024424.5:c.161G>C