Canonical Allele Identifier: PA915996648
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 487505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Arg238Trp
CA375714555
NM_001185091.2:c.712C>T