Canonical Allele Identifier: PA2829998808
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945795
ClinVar RCV Id: RCV003803889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro33Gln
CA379966391
NM_024424.5:c.98C>A