Canonical Allele Identifier: PA2825160920
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Val167Ile
CA379964871
NM_000378.6:c.499G>A