Canonical Allele Identifier: PA2826579239
Gene: GRM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 447467
ClinVar RCV Id: RCV000517333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264994.1:p.Ser17Phe
CA365956893
NM_001278065.2:c.50C>T