Canonical Allele Identifier: PA645374178
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 426563
ClinVar RCV Id: RCV000489124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser312Asn
CA384053113
NM_000834.3:c.935G>A