Canonical Allele Identifier: PA913198064
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 592388
ClinVar RCV Id: RCV000727630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_015566.1:p.Phe589Leu
CA375718896
NM_007327.4:c.1765T>C
CA375718912
NM_007327.4:c.1767C>A
CA375718915
NM_007327.4:c.1767C>G