Canonical Allele Identifier: PA915988881
Gene: LFNG HGNC NCBI

Linked Data

ClinVar Variation Id: 6999

Amino-acid Alleles

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