Canonical Allele Identifier: PA2573063746
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1319389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly96Arg
CA384054075
NM_000834.3:c.286G>C
CA384054077
NM_000834.3:c.286G>A