Canonical Allele Identifier: PA2573063747
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1303630
ClinVar RCV Id: RCV001763088 RCV002032787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser520Leu
CA384051877
NM_000834.3:c.1559C>T