Canonical Allele Identifier: PA315049
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205710
ClinVar RCV Id: RCV000187697 RCV000495871 RCV001172368 RCV001265244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Val620Met
CA315048
NM_000834.3:c.1858G>A