Canonical Allele Identifier: PA2580120788
Gene: GRIN2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1719565
ClinVar RCV Id: RCV002303819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000827.2:p.Gly624Ser
CA406697630
NM_000836.2:c.1870G>A