Allele Registry

Canonical Allele Identifier: PA119416

Gene: CCR2 HGNC NCBI

ClinVar RCV:

RCV000008756

RCV003982833

ClinVar Variation:

8267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116513.2:p.Val64Ile	CA119415 NM_001123041.3:c.190G>A