Canonical Allele Identifier: PA2826079704
Gene: CX3CR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 120091
ClinVar RCV Id: RCV000106289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164642.1:p.Phe262Ser
CA230620
NM_001171171.2:c.785T>C