Canonical Allele Identifier: PA916035806
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gln230Lys
CA8416347
NM_001353229.2:c.688C>A