Canonical Allele Identifier: PA915996749
Gene: GRIN1 HGNC NCBI
ClinVar RCV:
RCV000486798
ClinVar Variation:
421935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Ile663Leu
CA16618810
NM_001185091.2:c.1987A>C