Canonical Allele Identifier: PA645374140
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 411112
ClinVar RCV Id: RCV000460411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Cys8Ser
CA16613940
NM_000834.3:c.23G>C
CA384055157
NM_000834.3:c.22T>A