Canonical Allele Identifier: PA230621
Gene: CX3CR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 120091
ClinVar RCV Id: RCV000106289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164645.1:p.Phe294Ser
CA230620
NM_001171174.1:c.881T>C