Canonical Allele Identifier: PA891856844
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 569867
ClinVar RCV Id: RCV000690599 RCV001330053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly1436Ala
CA383985493
NM_000834.3:c.4307G>C