Canonical Allele Identifier: PA2830283948
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1382190
ClinVar RCV Id: RCV001897483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Leu25Met
CA398535384
NM_144606.7:c.73C>A