Canonical Allele Identifier: PA2830264165
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2681943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ile375Thr
CA398532278
NM_144997.7:c.1124T>C