Canonical Allele Identifier: PA2830284268
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1319112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Glu146Asp
CA398534564
NM_144606.7:c.438G>T
CA398534565
NM_144606.7:c.438G>C