Canonical Allele Identifier: PA2827720444
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala225Thr
CA8416341
NM_001353230.2:c.673G>A