Canonical Allele Identifier: PA2830000548
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Asp469Gly
CA016344
NM_024424.5:c.1406A>G