Canonical Allele Identifier: PA645374201
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 374243
ClinVar RCV Id: RCV000414971 RCV000500367 RCV000988791 RCV001265247 RCV002252116 RCV003324745 RCV003766167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Val558Ile
CA16043628
NM_000834.3:c.1672G>A