Canonical Allele Identifier: PA2830284260
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 388510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Phe143Leu
CA16608387
NM_144606.7:c.429C>G
CA398534585
NM_144606.7:c.429C>A
CA398534590
NM_144606.7:c.427T>C