Canonical Allele Identifier: PA915975952
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 39662
ClinVar RCV Id: RCV000032866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Leu649Val
CA130441
NM_001134408.2:c.1945C>G