Canonical Allele Identifier: PA2826154935
Gene: GRIN1 HGNC NCBI
ClinVar RCV:
RCV000484949
ClinVar Variation:
421469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172019.1:p.Pro553His
CA16618808
NM_001185090.2:c.1658C>A