Canonical Allele Identifier: PA2827721281
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1059893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ser575Leu
CA8415908
NM_001353230.2:c.1724C>T