Canonical Allele Identifier: PA2829977106
Gene: GRIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 592388
ClinVar RCV Id: RCV000727630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067544.1:p.Phe589Leu
CA375718896
NM_021569.4:c.1765T>C
CA375718912
NM_021569.4:c.1767C>A
CA375718915
NM_021569.4:c.1767C>G