Canonical Allele Identifier: PA2827721410
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 639059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ala45Glu
CA398535258
NM_001353231.2:c.134C>A