Canonical Allele Identifier: PA2829999257
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro131Ser
CA219511084
NM_024424.5:c.391C>T