Canonical Allele Identifier: PA1139686525
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 935441
ClinVar RCV Id: RCV001204033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Tyr312Asp
CA394798190
NM_001134408.2:c.934T>G