Canonical Allele Identifier: PA1139686776
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 995988
ClinVar RCV Id: RCV001290247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Asn693Asp
CA394797860
NM_001134408.2:c.2077A>G