Canonical Allele Identifier: PA2827721436
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg57Gln
CA8416509
NM_001353231.2:c.170G>A