Canonical Allele Identifier: PA2499234297
Gene: GRIN2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1013174
ClinVar RCV Id: RCV001311541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000827.2:p.Met681Val
CA406698345
NM_000836.2:c.2041A>G