Canonical Allele Identifier: PA2580119988
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1701006
ClinVar RCV Id: RCV002275881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Pro10His
CA233148023
NM_000834.3:c.29C>A