Canonical Allele Identifier: PA645374206
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 374327
ClinVar RCV Id: RCV000414856
ClinVar Variation Id: 916606
ClinVar RCV Id: RCV001172362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Trp607Cys
CA16043678
NM_000834.3:c.1821G>C
CA384051272
NM_000834.3:c.1821G>T