Canonical Allele Identifier: PA658676819
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 486528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Thr411Met
CA5667904
NM_016169.4:c.1232C>T