Canonical Allele Identifier: PA2573172060
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1422381
ClinVar RCV Id: RCV001919509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asp447Glu
CA384052397
NM_000834.3:c.1341C>G
CA384052398
NM_000834.3:c.1341C>A