Canonical Allele Identifier: PA2827720784
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2681943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ile375Thr
CA398532278
NM_001353230.2:c.1124T>C