Canonical Allele Identifier: PA204590
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 208643
ClinVar RCV Id: RCV000190648 RCV000235569 RCV000464558 RCV000791283 RCV001265246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly820Ala
CA204589
NM_000834.3:c.2459G>C