Canonical Allele Identifier: PA1139682774
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 835834
ClinVar RCV Id: RCV001036814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala509Thr
CA384051952
NM_000834.3:c.1525G>A