Canonical Allele Identifier: PA645374336
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 435384
ClinVar RCV Id: RCV000503060 RCV001522689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala1412Glu
CA383985888
NM_000834.3:c.4235C>A