Canonical Allele Identifier: PA2573203579
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1352848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro332Gln
CA8416191
NM_001353229.2:c.995C>A