Canonical Allele Identifier: PA2827720638
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2090606
ClinVar RCV Id: RCV003013189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu315Gln
CA398532954
NM_001353230.2:c.943G>C