Canonical Allele Identifier: PA645482330
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 406398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Thr353Met
CA5667865
NM_016169.4:c.1058C>T