Canonical Allele Identifier: PA2828455093
Gene: GRM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161472
ClinVar RCV Id: RCV000149006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358016.1:p.Arg647Cys
CA174098
NM_001371087.1:c.1939C>T