Canonical Allele Identifier: PA2828818157
Gene: COG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2914898
ClinVar RCV Id: RCV003609868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366195.1:p.Asp45His
CA8134050
NM_001379266.1:c.133G>C