Canonical Allele Identifier: PA2573172073
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1485071
ClinVar RCV Id: RCV002008382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly611Arg
CA384051249
NM_000834.3:c.1831G>C