Canonical Allele Identifier: PA2830264882
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2993792
ClinVar RCV Id: RCV003853367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys551Gln
CA398529937
NM_144997.7:c.1651A>C