Canonical Allele Identifier: PA2825236815
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2930429
ClinVar RCV Id: RCV003789739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Arg67Trp
CA233148010
NM_000834.3:c.199C>T