Canonical Allele Identifier: PA2499234212
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1285562
ClinVar RCV Id: RCV001706919 RCV003771861 RCV004526140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ile240Val
CA384053736
NM_000834.3:c.718A>G