Canonical Allele Identifier: PA645374184
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 279975
ClinVar RCV Id: RCV000317346 RCV000655320 RCV001172351 RCV001265472 RCV001723869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Asn516Ser
CA10603239
NM_000834.3:c.1547A>G