Canonical Allele Identifier: PA915996809
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208743
ClinVar Variation Id: 1452432
ClinVar RCV Id: RCV001999807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Gly836Arg
CA204805
NM_001185091.2:c.2506G>A
CA375726017
NM_001185091.2:c.2506G>C