Canonical Allele Identifier: PA1139682568
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 985796
ClinVar RCV Id: RCV001266887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Met132Ile
CA384053494
NM_000834.3:c.396G>T
CA384053496
NM_000834.3:c.396G>C
CA384053498
NM_000834.3:c.396G>A