Canonical Allele Identifier: PA2741822557
Gene: GRIN2D HGNC NCBI

Linked Data

ClinVar Variation Id: 3000273
ClinVar RCV Id: RCV003857448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000827.2:p.Val647Met
CA406697964
NM_000836.2:c.1939G>A