Canonical Allele Identifier: PA2829999266
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937351
ClinVar RCV Id: RCV003791541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro133Gln
CA379965781
NM_024424.5:c.398C>A