Canonical Allele Identifier: PA2573063745
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1312242
ClinVar RCV Id: RCV001754996 RCV003772017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser22Ala
CA384055072
NM_000834.3:c.64T>G
CA2573053638
NM_000834.3:c.63_64delinsTG