Canonical Allele Identifier: PA225882
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 98465
ClinVar RCV Id: RCV000084756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000824.1:p.Asn886Ser
CA225881
NM_000833.5:c.2657A>G