Canonical Allele Identifier: PA2825779000
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1524938
ClinVar RCV Id: RCV002032086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Asn886Lys
CA394709637
NM_001134407.3:c.2658T>G
CA394709638
NM_001134407.3:c.2658T>A