Canonical Allele Identifier: PA2827720037
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1519156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ser68Arg
CA398535108
NM_001353230.2:c.204C>G
CA398535109
NM_001353230.2:c.204C>A
CA398535114
NM_001353230.2:c.202A>C