Canonical Allele Identifier: PA2827346772
Gene: CX3CR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 120091
ClinVar RCV Id: RCV000106289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001328.1:p.Phe262Ser
CA230620
NM_001337.4:c.785T>C