Canonical Allele Identifier: PA102714
Gene: NOG HGNC NCBI

Linked Data

ClinVar Variation Id: 6691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005441.1:p.Tyr222Cys
CA118425
NM_005450.6:c.665A>G