Canonical Allele Identifier: PA916008811
Gene: GRM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 447467
ClinVar RCV Id: RCV000517333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264996.1:p.Ser17Phe
CA365956893
NM_001278067.1:c.50C>T