Canonical Allele Identifier: PA2580390776
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1753905
ClinVar RCV Id: RCV002364136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057253.2:p.Ala22Ser
CA377886319
NM_016169.4:c.64G>T