Canonical Allele Identifier: PA1139682744
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 916598
ClinVar RCV Id: RCV001172348 RCV002379671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Cys461Phe
CA384052299
NM_000834.3:c.1382G>T