Canonical Allele Identifier: PA2827720238
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1370294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly144Arg
CA288317171
NM_001353230.2:c.430G>A
CA398534584
NM_001353230.2:c.430G>C