Canonical Allele Identifier: PA1139710688
Gene: NOG HGNC NCBI

Linked Data

ClinVar Variation Id: 871465
ClinVar RCV Id: RCV001091452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005441.1:p.Ser231Pro
CA399966994
NM_005450.6:c.691T>C