Canonical Allele Identifier: PA1139682644
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 838589
ClinVar RCV Id: RCV001040168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser320Gly
CA384053056
NM_000834.3:c.958A>G