Canonical Allele Identifier: PA658664508
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg392Gln
CA8416129
NM_144997.7:c.1175G>A