Canonical Allele Identifier: PA645374240
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 234527
ClinVar RCV Id: RCV000222391 RCV001172326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala734Val
CA10577447
NM_000834.3:c.2201C>T