Canonical Allele Identifier: PA2573203669
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1462596
ClinVar RCV Id: RCV001954301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Val399del
CA2573153080
NM_001353229.2:c.1196_1198del