Canonical Allele Identifier: PA2825237246
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2432299
ClinVar RCV Id: RCV003131077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asp286Gly
CA384053288
NM_000834.3:c.857A>G