Canonical Allele Identifier: PA915996659
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 663888
ClinVar RCV Id: RCV000821857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Asp324Tyr
CA375715139
NM_001185091.2:c.970G>T