Canonical Allele Identifier: PA2825236895
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2083725
ClinVar RCV Id: RCV003002754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gln105Glu
CA6461433
NM_000834.3:c.313C>G