Canonical Allele Identifier: PA174100
Gene: GRM8 HGNC NCBI

Linked Data

ClinVar Variation Id: 161472
ClinVar RCV Id: RCV000149006
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120795.1:p.Arg852Cys
CA174098
NM_001127323.1:c.2554C>T