Canonical Allele Identifier: PA2499234262
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1009295
ClinVar RCV Id: RCV001306762 RCV001330051
ClinVar Variation Id: 2938708
ClinVar RCV Id: RCV003799482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Gly1002Arg
CA6460955
NM_000834.3:c.3004G>C
CA6460956
NM_000834.3:c.3004G>A