Canonical Allele Identifier: PA2826197793
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_001182068.2:p.Ser689Trp
CA396578416
NM_001195139.2:c.2066C>G