Canonical Allele Identifier: PA2825237279
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1918101
ClinVar RCV Id: RCV002601793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.His325Tyr
CA6461350
NM_000834.3:c.973C>T