Canonical Allele Identifier: PA2573301101
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1496182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg17Cys
CA8416533
NM_144997.7:c.49C>T