Canonical Allele Identifier: PA357907
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 224818
ClinVar RCV Id: RCV000210391 RCV000478281 RCV001004753 RCV001265248 RCV003126605 RCV001853372 RCV004017491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly689Ser
CA357906
NM_000834.3:c.2065G>A