Canonical Allele Identifier: PA915996669
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 493503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Thr391Ala
CA375715596
NM_001185091.2:c.1171A>G