Canonical Allele Identifier: PA2827721248
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 480818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.His564Tyr
CA398529843
NM_001353230.2:c.1690C>T