Canonical Allele Identifier: PA645374174
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 432918
ClinVar RCV Id: RCV000497849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala244Ser
CA384053689
NM_000834.3:c.730G>T