Canonical Allele Identifier: PA645374193
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 397525
ClinVar RCV Id: RCV000449489 RCV002522738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly533Asp
CA16609402
NM_000834.3:c.1598G>A