Canonical Allele Identifier: PA2499234239
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1298538
ClinVar RCV Id: RCV001726868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asp113Asn
CA384053781
NM_000834.3:c.337G>A