Canonical Allele Identifier: PA2829998726
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718400
ClinVar RCV Id: RCV002304892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala18Ser
CA379966487
NM_024424.5:c.52G>T