Canonical Allele Identifier: PA314995
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 205681
ClinVar RCV Id: RCV000187668 RCV000639586 RCV001281433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000824.1:p.Glu1321Gln
CA314994
NM_000833.5:c.3961G>C