Canonical Allele Identifier: PA645374177
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 426490
ClinVar RCV Id: RCV000490109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser281Thr
CA384053329
NM_000834.3:c.841T>A