Canonical Allele Identifier: PA645374176
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 377943
ClinVar RCV Id: RCV001398757 RCV001712192 RCV002318388 RCV004530536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala271Val
CA6461362
NM_000834.3:c.812C>T