Canonical Allele Identifier: PA2830284261
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1370294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Gly144Arg
CA288317171
NM_144606.7:c.430G>A
CA398534584
NM_144606.7:c.430G>C