Canonical Allele Identifier: PA2827719293
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gly34Glu
CA398535333
NM_001353229.2:c.101G>A