Canonical Allele Identifier: PA2825879696
Gene: COG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 806379
ClinVar RCV Id: RCV000994280 RCV001244953 RCV004030170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138508.1:p.Arg356Trp
CA1447655
NM_001145036.2:c.1066C>T