Canonical Allele Identifier: PA891851689
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 573218
ClinVar RCV Id: RCV000694830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Glu3Gly
CA5667574
NM_016169.4:c.8A>G