Canonical Allele Identifier: PA2825237521
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2939828
ClinVar RCV Id: RCV003794994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Met503Ile
CA384051991
NM_000834.3:c.1509G>T
CA384051992
NM_000834.3:c.1509G>C
CA384051993
NM_000834.3:c.1509G>A