Canonical Allele Identifier: PA915975592
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 211118
ClinVar RCV Id: RCV000194066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.His1361Asp
CA207978
NM_001134407.3:c.4081C>G