Canonical Allele Identifier: PA2825238722
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2942365
ClinVar RCV Id: RCV003805579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asp1047Asn
CA383990735
NM_000834.3:c.3139G>A