Canonical Allele Identifier: PA2825778806
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1016692
ClinVar RCV Id: RCV001315731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.His674Gln
CA278179185
NM_001134407.3:c.2022T>G
CA394797977
NM_001134407.3:c.2022T>A