Allele Registry

Canonical Allele Identifier: PA2573076071

Gene: COG8 HGNC NCBI

ClinVar Allele:

102113

ClinVar RCV:

RCV000082298

RCV000723761

RCV001317887

RCV003964945

ClinVar Variation:

96219

HGVS (amino-acid)	Matching Registered Transcripts
NP_001366190.1:p.Thr608Met	CA223835 NM_001379261.1:c.1823C>T