Canonical Allele Identifier: PA2825879737
Gene: COG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 417771
ClinVar RCV Id: RCV000477726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138508.1:p.Trp633Gly
CA345198944
NM_001145036.2:c.1897T>G