Allele Registry

Canonical Allele Identifier: PA2826155052

Gene: GRIN1 HGNC NCBI

ClinVar RCV:

RCV000442420

ClinVar Variation:

376787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001172019.1:p.Pro691Thr	CA16603167 NM_001185090.2:c.2071C>A