Canonical Allele Identifier: PA2827721340
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 851074
ClinVar RCV Id: RCV001055395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu19Pro
CA398535419
NM_001353231.2:c.56T>C