Canonical Allele Identifier: PA2830264211
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1717584
ClinVar RCV Id: RCV002296475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Val384Leu
CA398532186
NM_144997.7:c.1150G>C