Canonical Allele Identifier: PA2825161622
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.His433Tyr
CA016298
NM_000378.6:c.1297C>T