Allele Registry

Canonical Allele Identifier: PA645374248

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000414776

ClinVar Variation:

373959

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Gly799Ser	CA16043466 NM_000834.3:c.2395G>A