Canonical Allele Identifier: PA2580211250
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2418071
ClinVar RCV Id: RCV003118180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu311Lys
CA398533109
NM_001353229.2:c.931G>A