Canonical Allele Identifier: PA916036006
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 229915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg588His
CA8415911
NM_001353229.2:c.1763G>A