Canonical Allele Identifier: PA891856714
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 583000
ClinVar RCV Id: RCV000707216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Leu308Pro
CA384053142
NM_000834.3:c.923T>C