Canonical Allele Identifier: PA915975674
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 502679
ClinVar RCV Id: RCV000597548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Ala136Ser
CA394715062
NM_001134408.2:c.406G>T