Canonical Allele Identifier: PA2827719863
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229241
ClinVar RCV Id: RCV004524820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu594Gln
CA398529775
NM_001353229.2:c.1780G>C