Canonical Allele Identifier: PA2573063748
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1302119
ClinVar RCV Id: RCV001754008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Pro122Leu
CA384053634
NM_000834.3:c.365C>T
CA2573053637
NM_000834.3:c.365_366delinsTG