Allele Registry

Canonical Allele Identifier: PA645374206

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000414856

RCV001172362

ClinVar Variation:

374327

916606

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Trp607Cys	CA16043678 NM_000834.3:c.1821G>C CA384051272 NM_000834.3:c.1821G>T