Canonical Allele Identifier: PA2825234980
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1131651
ClinVar RCV Id: RCV001465594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000824.1:p.Tyr676Ser
CA394797966
NM_000833.5:c.2027A>C