Allele Registry

Canonical Allele Identifier: PA094650

Gene: LFNG HGNC NCBI

ClinVar Variation Id: 6999

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035257.1:p.Phe188Leu	CA340626 NM_001040167.2:c.564C>A CA366617018 NM_001040167.2:c.562T>C CA366617030 NM_001040167.2:c.564C>G