Canonical Allele Identifier: PA2499234221
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1189076
ClinVar RCV Id: RCV001549336 RCV002570682 RCV004039292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gln331Lys
CA384052977
NM_000834.3:c.991C>A