Canonical Allele Identifier: PA2828817838
Gene: COG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516557
ClinVar RCV Id: RCV002040869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366192.1:p.Gly340Ser
CA8133803
NM_001379263.1:c.1018G>A