Canonical Allele Identifier: PA2499234287
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1010999
ClinVar RCV Id: RCV001308732 RCV004034181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly1370Arg
CA6460783
NM_000834.3:c.4108G>A
CA383986556
NM_000834.3:c.4108G>C