Canonical Allele Identifier: PA645478701
Gene: TREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356675
ClinVar RCV Id: RCV000405068 RCV002058608 RCV003912526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258750.1:p.Val166Met
CA3798803
NM_001271821.2:c.496G>A