Canonical Allele Identifier: PA1139687253
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 859074
ClinVar RCV Id: RCV001065099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Asp1131Glu
CA394707962
NM_001134408.2:c.3393T>G
CA394707963
NM_001134408.2:c.3393T>A