Canonical Allele Identifier: PA2827719278
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 567066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu29Pro
CA8416519
NM_001353229.2:c.86T>C