Canonical Allele Identifier: PA2825236719
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1982082
ClinVar RCV Id: RCV002794942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser9Pro
CA6461474
NM_000834.3:c.25T>C