Canonical Allele Identifier: PA915975584
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 807985
ClinVar RCV Id: RCV000996201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Ser1330Thr
CA394706409
NM_001134407.3:c.3989G>C