Canonical Allele Identifier: PA2573076071
Gene: COG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 96219

Amino-acid Alleles

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