Canonical Allele Identifier: PA2825236939
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2922197
ClinVar RCV Id: RCV003785411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Leu124Val
CA384053612
NM_000834.3:c.370C>G