Canonical Allele Identifier: PA645374164
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 245940
ClinVar RCV Id: RCV000235741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ile126Thr
CA10584429
NM_000834.3:c.377T>C