Canonical Allele Identifier: PA915976127
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 205661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Arg899Trp
CA314954
NM_001134408.2:c.2695C>T