Canonical Allele Identifier: PA658809532
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg57Gln
CA8416509
NM_144997.7:c.170G>A