Canonical Allele Identifier: PA2825237726
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2937095
ClinVar RCV Id: RCV003791285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly603Ser
CA384051303
NM_000834.3:c.1807G>A