Canonical Allele Identifier: PA2830264836
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2896183
ClinVar RCV Id: RCV003608611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu543Gln
CA398529989
NM_144997.7:c.1627G>C