Canonical Allele Identifier: PA2825236922
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2937751
ClinVar RCV Id: RCV003794381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Thr121Ile
CA384053643
NM_000834.3:c.362C>T