Canonical Allele Identifier: PA2830264267
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro396His
CA398531989
NM_144997.7:c.1187C>A