Canonical Allele Identifier: PA2573292221
Gene: COG8 HGNC NCBI
ClinVar RCV:
RCV002040869
ClinVar Variation:
1516557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115758.3:p.Gly340Ser
CA8133803
NM_032382.5:c.1018G>A