Canonical Allele Identifier: PA2829999441
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2949798
ClinVar RCV Id: RCV003804964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Phe169Ser
CA379964844
NM_024424.5:c.506T>C