Canonical Allele Identifier: PA2827721287
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229241
ClinVar RCV Id: RCV004524820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu576Gln
CA398529775
NM_001353230.2:c.1726G>C