Canonical Allele Identifier: PA2828817972
Gene: COG8 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366193.1:p.Gly340Ser
CA8133803
NM_001379264.1:c.1018G>A