Canonical Allele Identifier: PA2827722429
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 230541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu455Gly
CA8416016
NM_001353231.2:c.1364A>G