Canonical Allele Identifier: PA2827719415
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 649173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Lys78Arg
CA398535046
NM_001353229.2:c.233A>G