Canonical Allele Identifier: PA915996829
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 433116
ClinVar RCV Id: RCV000656029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Ile856Thr
CA375726637
NM_001185091.2:c.2567T>C