Canonical Allele Identifier: PA915996776
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 813929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Pro681Leu
CA375721205
NM_001185091.2:c.2042C>T