Canonical Allele Identifier: PA2825778808
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1131651
ClinVar RCV Id: RCV001465594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Tyr676Ser
CA394797966
NM_001134407.3:c.2027A>C