Canonical Allele Identifier: PA2827719985
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 187016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu47Gln
CA196505
NM_001353230.2:c.139G>C