Canonical Allele Identifier: PA2580156437
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801079
ClinVar RCV Id: RCV002462676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Asn911Tyr
CA394709475
NM_001134408.2:c.2731A>T