Canonical Allele Identifier: PA2825237191
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1762316
ClinVar RCV Id: RCV002427812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Phe273Val
CA384053375
NM_000834.3:c.817T>G