Canonical Allele Identifier: PA2825237184
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2432293
ClinVar RCV Id: RCV003135471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Val269Leu
CA384053405
NM_000834.3:c.805G>T
CA384053408
NM_000834.3:c.805G>C