Canonical Allele Identifier: PA915996660
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450075
ClinVar RCV Id: RCV000521029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Lys337Arg
CA375715227
NM_001185091.2:c.1010A>G