Canonical Allele Identifier: PA915996782
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429761
ClinVar RCV Id: RCV000494405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Ser709Pro
CA375722032
NM_001185091.2:c.2125T>C