Canonical Allele Identifier: PA2825237672
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2950630
ClinVar RCV Id: RCV003809940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Phe577Leu
CA384051482
NM_000834.3:c.1731T>G
CA384051483
NM_000834.3:c.1731T>A
CA384051488
NM_000834.3:c.1729T>C