Canonical Allele Identifier: PA2825236994
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2954226
ClinVar RCV Id: RCV003813449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ile133Val
CA384053485
NM_000834.3:c.397A>G