Canonical Allele Identifier: PA2827721256
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 993694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Met566Thr
CA8415916
NM_001353230.2:c.1697T>C