Canonical Allele Identifier: PA916035903
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg419Cys
CA8416096
NM_001353229.2:c.1255C>T