Canonical Allele Identifier: PA2828818012
Gene: COG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 96219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366193.1:p.Thr561Met
CA223835
NM_001379264.1:c.1682C>T