Canonical Allele Identifier: PA2829976705
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1810652
ClinVar RCV Id: RCV002510139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067544.1:p.Phe321Cys
CA375715260
NM_021569.4:c.962T>G