Canonical Allele Identifier: PA2827721701
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1715285
ClinVar RCV Id: RCV002304521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ile158Leu
CA398534484
NM_001353231.2:c.472A>C