Canonical Allele Identifier: PA315063
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205717
ClinVar RCV Id: RCV000187704 RCV003765191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ser1033Arg
CA315062
NM_000834.3:c.3099C>G
CA383990977
NM_000834.3:c.3099C>A
CA383990994
NM_000834.3:c.3097A>C