Canonical Allele Identifier: PA915965428
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 699210
ClinVar RCV Id: RCV001447365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Arg84Cys
CA384054242
NM_000834.3:c.250C>T