Canonical Allele Identifier: PA916035875
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 581992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu374Val
CA8416144
NM_001353229.2:c.1120C>G