Canonical Allele Identifier: PA915975597
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 392394
ClinVar RCV Id: RCV000423593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Pro1366Ser
CA16607504
NM_001134407.3:c.4096C>T