Canonical Allele Identifier: PA2829999460
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679631
ClinVar RCV Id: RCV003464888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala177Asp
CA379964762
NM_024424.5:c.530C>A