Canonical Allele Identifier: PA916035944
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 230541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu473Gly
CA8416016
NM_001353229.2:c.1418A>G