Canonical Allele Identifier: PA2499251458
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1041689
ClinVar RCV Id: RCV001345530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Lys566Thr
CA398529951
NM_001353229.2:c.1697A>C