Allele Registry

Canonical Allele Identifier: PA111447

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000022582

RCV001260642

RCV001541943

ClinVar Variation:

29730

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Arg682Cys	CA128599 NM_000834.3:c.2044C>T