Canonical Allele Identifier: PA915975942
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 432031
ClinVar RCV Id: RCV000497833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Thr646Arg
CA394799337
NM_001134408.2:c.1937C>G