Canonical Allele Identifier: PA2573076069
Gene: COG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 235232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366190.1:p.Pro578Ser
CA8133644
NM_001379261.1:c.1732C>T