Allele Registry

Canonical Allele Identifier: PA915988881

Gene: LFNG HGNC NCBI

ClinVar Variation Id: 6999

HGVS (amino-acid)	Matching Registered Transcripts
NP_002295.1:p.Phe59Leu	CA340626 NM_002304.3:c.177C>A CA366617018 NM_002304.3:c.175T>C CA366617030 NM_002304.3:c.177C>G