Canonical Allele Identifier: PA2499234215
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1041088
ClinVar RCV Id: RCV001344834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Thr268Pro
CA233115839
NM_000834.3:c.802A>C