Canonical Allele Identifier: PA2825778825
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2811707
ClinVar RCV Id: RCV003741727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Asn693Lys
CA394797853
NM_001134407.3:c.2079C>G
CA394797854
NM_001134407.3:c.2079C>A