Canonical Allele Identifier: PA2826155219
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 539838
ClinVar RCV Id: RCV000649655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Arg52Gly
CA375713258
NM_001185091.2:c.154C>G