Canonical Allele Identifier: PA174338
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161558
ClinVar RCV Id: RCV000149093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_015566.1:p.Pro117Leu
CA174336
NM_007327.4:c.350C>T