Canonical Allele Identifier: PA2830264861
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1041689
ClinVar RCV Id: RCV001345530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys548Thr
CA398529951
NM_144997.7:c.1643A>C