Canonical Allele Identifier: PA2829998944
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2925823
ClinVar RCV Id: RCV003783917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg61Gln
CA379966214
NM_024424.5:c.182G>A