Canonical Allele Identifier: PA2828803943
Gene: GRIA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098705
ClinVar RCV Id: RCV001420668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365929.3:p.Leu200Val
CA358646141
NM_001379000.3:c.598C>G