Canonical Allele Identifier: PA2825160937
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 933906
ClinVar RCV Id: RCV001202216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr176Ile
CA379964768
NM_000378.6:c.527C>T