Allele Registry

Canonical Allele Identifier: PA2499234286

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV001519000

ClinVar Variation:

1168612

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Asn1365His	CA383986626 NM_000834.3:c.4093A>C