Canonical Allele Identifier: PA2826539809
Gene: TREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5215
ClinVar RCV Id: RCV000005525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258750.1:p.Asp134Gly
CA253436
NM_001271821.2:c.401A>G