Canonical Allele Identifier: PA2827719975
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 651581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly42Arg
CA398535280
NM_001353230.2:c.124G>C