Canonical Allele Identifier: PA2826224414
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Asp235Gly
CA016344
NM_001198552.2:c.704A>G