Canonical Allele Identifier: PA915965562
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 660295
ClinVar RCV Id: RCV000817460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Leu1424Phe
CA6460754
NM_000834.3:c.4270C>T