Canonical Allele Identifier: PA2580120032
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1701895
ClinVar RCV Id: RCV002277699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Val523Ala
CA384051858
NM_000834.3:c.1568T>C