Canonical Allele Identifier: PA2830263343
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2675745
ClinVar RCV Id: RCV003461589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gly139Ser
CA398534616
NM_144997.7:c.415G>A