Canonical Allele Identifier: PA1139682761
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 916069
ClinVar RCV Id: RCV001171570 RCV001172349 RCV001809986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly499Arg
CA384052035
NM_000834.3:c.1495G>C
CA384052036
NM_000834.3:c.1495G>A