Canonical Allele Identifier: PA315063
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205717

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