Canonical Allele Identifier: PA2825236785
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2584970
ClinVar RCV Id: RCV003340870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ala53Ser
CA384054734
NM_000834.3:c.157G>T