Allele Registry

Canonical Allele Identifier: PA102692

Gene: NOG HGNC NCBI

ClinVar RCV:

RCV000007081

ClinVar Variation:

6693

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