Canonical Allele Identifier: PA2826155069
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422175
ClinVar RCV Id: RCV001926069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172019.1:p.Met723Thr
CA375722251
NM_001185090.2:c.2168T>C