Canonical Allele Identifier: PA2830284541
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1921452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Ala259Thr
CA398533824
NM_144606.7:c.775G>A