Allele Registry

Canonical Allele Identifier: PA2825879737

Gene: COG2 HGNC NCBI

ClinVar RCV:

RCV000477726

ClinVar Variation:

417771

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138508.1:p.Trp633Gly	CA345198944 NM_001145036.2:c.1897T>G