Canonical Allele Identifier: PA196507
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 187016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu47Gln
CA196505
NM_144997.7:c.139G>C