Canonical Allele Identifier: PA2826140627
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2586928
ClinVar RCV Id: RCV003360698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Gly11Val
CA377886160
NM_001178133.2:c.32G>T