Canonical Allele Identifier: PA915996690
Gene: GRIN1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Pro553His
CA16618808
NM_001185091.2:c.1658C>A