Canonical Allele Identifier: PA891863769
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala10Asp
CA379966534
NM_024426.6:c.29C>A