Canonical Allele Identifier: PA210140
Gene: GRID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208923
ClinVar RCV Id: RCV000201339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060021.1:p.Arg148Cys
CA210139
NM_017551.3:c.442C>T