Canonical Allele Identifier: PA2580120022
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1708932
ClinVar RCV Id: RCV002288216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Glu443Asp
CA233011183
NM_000834.3:c.1329G>C
CA384052425
NM_000834.3:c.1329G>T