Canonical Allele Identifier: PA102692
Gene: NOG HGNC NCBI

Linked Data

ClinVar Variation Id: 6693
ClinVar RCV Id: RCV000007081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005441.1:p.Trp217Gly
CA118427
NM_005450.6:c.649T>G