Canonical Allele Identifier: PA2825236857
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2076159
ClinVar RCV Id: RCV002972176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ile82Val
CA384054265
NM_000834.3:c.244A>G