Canonical Allele Identifier: PA915996774
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Arg680Trp
CA16621877
NM_001185091.2:c.2038C>T