Canonical Allele Identifier: PA2825237277
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2574918
ClinVar RCV Id: RCV003319815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asn323Lys
CA384053028
NM_000834.3:c.969C>G
CA384053029
NM_000834.3:c.969C>A