Canonical Allele Identifier: PA915976199
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 665830
ClinVar RCV Id: RCV000824198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Val1000Met
CA394708891
NM_001134408.2:c.2998G>A