Canonical Allele Identifier: PA2830284031
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Arg57Gln
CA8416509
NM_144606.7:c.170G>A