Canonical Allele Identifier: PA915965450
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 806838
ClinVar RCV Id: RCV000994859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly603Arg
CA384051305
NM_000834.3:c.1807G>C