Canonical Allele Identifier: PA2826140614
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 1369018
ClinVar RCV Id: RCV001874556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171604.1:p.Ser7Gly
CA377886106
NM_001178133.2:c.19A>G