Canonical Allele Identifier: PA2825778813
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2500345
ClinVar RCV Id: RCV003225003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Gly683Arg
CA394797923
NM_001134407.3:c.2047G>C
CA394797924
NM_001134407.3:c.2047G>A