Canonical Allele Identifier: PA2825236951
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2499406
ClinVar RCV Id: RCV003221707 RCV003779797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser131Phe
CA384053512
NM_000834.3:c.392C>T