Canonical Allele Identifier: PA2573172076
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1394652
ClinVar RCV Id: RCV001900955 RCV003314706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala644Thr
CA384051016
NM_000834.3:c.1930G>A