Canonical Allele Identifier: PA2825778452
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000191
ClinVar RCV Id: RCV001296287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Ser311Phe
CA394798191
NM_001134407.3:c.932C>T