Canonical Allele Identifier: PA915975616
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 567877
ClinVar RCV Id: RCV000688073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Asn1420Ser
CA7896187
NM_001134407.3:c.4259A>G