Canonical Allele Identifier: PA2827721200
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1352071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ile538Leu
CA398530017
NM_001353230.2:c.1612A>C