Canonical Allele Identifier: PA2825161667
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Asp452Gly
CA016344
NM_000378.6:c.1355A>G