Canonical Allele Identifier: PA2826155040
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 422332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172019.1:p.Asp679Glu
CA16618812
NM_001185090.2:c.2037C>G
CA375721177
NM_001185090.2:c.2037C>A