Canonical Allele Identifier: PA645414286
Gene: COG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 417771
ClinVar RCV Id: RCV000477726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031383.1:p.Trp634Gly
CA345198944
NM_007357.3:c.1900T>G