Canonical Allele Identifier: PA340627
Gene: LFNG HGNC NCBI

Linked Data

ClinVar Variation Id: 6999
ClinVar RCV Id: RCV000007414 RCV002269818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035258.1:p.Phe188Leu
CA340626
NM_001040168.2:c.564C>A
CA366617018
NM_001040168.2:c.562T>C
CA366617030
NM_001040168.2:c.564C>G