Canonical Allele Identifier: PA2826155061
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429761
ClinVar RCV Id: RCV000494405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172019.1:p.Ser709Pro
CA375722032
NM_001185090.2:c.2125T>C