Canonical Allele Identifier: PA174099
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_000836.2:p.Arg852Cys
CA174098
NM_000845.3:c.2554C>T