Canonical Allele Identifier: PA891851693
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 582859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Gly11Asp
CA377886163
NM_016169.4:c.32G>A