Allele Registry

Canonical Allele Identifier: PA2829977552

Gene: GRIN1 HGNC NCBI

ClinVar RCV:

RCV002278859

ClinVar Variation:

1702541

HGVS (amino-acid)	Matching Registered Transcripts
NP_067544.1:p.Thr865Ser	CA375729537 NM_021569.4:c.2593A>T CA375729542 NM_021569.4:c.2594C>G