Canonical Allele Identifier: PA2825237044
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2943957
ClinVar RCV Id: RCV003803515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000825.2:p.Ile160Phe
CA384054702
NM_000834.3:c.478A>T