Canonical Allele Identifier: PA2829999465
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2941440
ClinVar RCV Id: RCV003795142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly178Arg
CA379964756
NM_024424.5:c.532G>C
CA379964758
NM_024424.5:c.532G>A