Canonical Allele Identifier: PA2829998647
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 998537
ClinVar RCV Id: RCV001294408
ClinVar Variation Id: 1022558
ClinVar RCV Id: RCV001322486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Asp8Glu
CA379966544
NM_024424.5:c.24C>G
CA379966545
NM_024424.5:c.24C>A