Canonical Allele Identifier: PA1139682619
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 849384
ClinVar RCV Id: RCV001053329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Pro290Ser
CA384053262
NM_000834.3:c.868C>T