Canonical Allele Identifier: PA2830264754
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 653093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys520Arg
CA8415935
NM_144997.7:c.1559A>G