Canonical Allele Identifier: PA2827720796
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1462596
ClinVar RCV Id: RCV001954301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Val381del
CA2573153080
NM_001353230.2:c.1142_1144del