Canonical Allele Identifier: PA916036003
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 480818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.His582Tyr
CA398529843
NM_001353229.2:c.1744C>T