Canonical Allele Identifier: PA915996777
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29725
ClinVar RCV Id: RCV000022577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Glu683Lys
CA128598
NM_001185091.2:c.2047G>A