Canonical Allele Identifier: PA2825237164
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 3061857
ClinVar RCV Id: RCV003984904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Cys232Arg
CA384053837
NM_000834.3:c.694T>C