Canonical Allele Identifier: PA2825239628
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2946308
ClinVar RCV Id: RCV003806594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Arg1422Gly
CA383985731
NM_000834.3:c.4264C>G