Canonical Allele Identifier: PA2573172052
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1468530
ClinVar RCV Id: RCV001970671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Thr250Ser
CA384053623
NM_000834.3:c.749C>G
CA384053624
NM_000834.3:c.748A>T