Canonical Allele Identifier: PA2828817750
Gene: COG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 96219
ClinVar RCV Id: RCV000082298 RCV000723761 RCV001317887 RCV003964945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366191.1:p.Thr561Met
CA223835
NM_001379262.1:c.1682C>T