Canonical Allele Identifier: PA2830000285
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg385Gln
CA016505
NM_024424.5:c.1154G>A