Canonical Allele Identifier: PA2830264261
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1742726
ClinVar RCV Id: RCV002335476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Leu395Ile
CA398532006
NM_144997.7:c.1183C>A