Canonical Allele Identifier: PA2741822553
Gene: GRIN2D HGNC NCBI

Linked Data

ClinVar Variation Id: 3031480
ClinVar RCV Id: RCV003897071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000827.2:p.Thr626Ser
CA406697661
NM_000836.2:c.1876A>T
CA406697665
NM_000836.2:c.1877C>G