Canonical Allele Identifier: PA1139682802
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 916600
ClinVar RCV Id: RCV001172352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Phe525Val
CA384051846
NM_000834.3:c.1573T>G