Canonical Allele Identifier: PA645374162
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 246440
ClinVar RCV Id: RCV000235573 RCV001033993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala109Ser
CA10584431
NM_000834.3:c.325G>T