Canonical Allele Identifier: PA2830264092
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Phe361Ser
CA398532372
NM_144997.7:c.1082T>C