Canonical Allele Identifier: PA2830264210
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 840448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Val384Ile
CA8416132
NM_144997.7:c.1150G>A