Canonical Allele Identifier: PA2825237114
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2948990
ClinVar RCV Id: RCV003801716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Phe182Leu
CA384054419
NM_000834.3:c.546T>G
CA384054421
NM_000834.3:c.546T>A
CA384054426
NM_000834.3:c.544T>C