Canonical Allele Identifier: PA916035990
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 819626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Thr550Pro
CA8415931
NM_001353229.2:c.1648A>C