Canonical Allele Identifier: PA2827719354
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 851547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg59Pro
CA398535164
NM_001353229.2:c.176G>C