Canonical Allele Identifier: PA2742011325
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Met58Thr
CA398535171
NM_144997.7:c.173T>C