Canonical Allele Identifier: PA2580161635
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720436
ClinVar RCV Id: RCV002298176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172020.1:p.Lys799Asn
CA375724904
NM_001185091.2:c.2397G>C
CA375724905
NM_001185091.2:c.2397G>T