Canonical Allele Identifier: PA2741957972
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2586928
ClinVar RCV Id: RCV003360698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Gly11Val
CA377886160
NM_016169.4:c.32G>T