Canonical Allele Identifier: PA2826539805
Gene: TREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258750.1:p.Val126Gly
CA340365
NM_001271821.2:c.377T>G