Canonical Allele Identifier: PA2830263906
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 654466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala310Thr
CA8416194
NM_144997.7:c.928G>A