Canonical Allele Identifier: PA915965463
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 657233
ClinVar RCV Id: RCV000813802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Phe709Val
CA383999053
NM_000834.3:c.2125T>G