Canonical Allele Identifier: PA2829999415
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365771
ClinVar RCV Id: RCV001929946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser163Asn
CA379964906
NM_024424.5:c.488G>A