Canonical Allele Identifier: PA2827721230
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1463495
ClinVar RCV Id: RCV001956647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Phe552Tyr
CA398529924
NM_001353230.2:c.1655T>A