Allele Registry

Canonical Allele Identifier: PA2499234249

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV001358743

ClinVar Variation:

1050841

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Leu781Met	CA383997990 NM_000834.3:c.2341C>A