Canonical Allele Identifier: PA111329
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 39662
ClinVar RCV Id: RCV000032866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000824.1:p.Leu649Val
CA130441
NM_000833.5:c.1945C>G