Canonical Allele Identifier: PA2828167027
Gene: COG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016153
ClinVar RCV Id: RCV001315117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352355.1:p.Ser572Trp
CA396578416
NM_001365426.1:c.1715C>G