Canonical Allele Identifier: PA2827721266
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 229915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg570His
CA8415911
NM_001353230.2:c.1709G>A