Canonical Allele Identifier: PA645374173
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 429966
ClinVar RCV Id: RCV000493024 RCV001085323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ile227Val
CA233115920
NM_000834.3:c.679A>G