Canonical Allele Identifier: PA2830283961
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 567066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Leu29Pro
CA8416519
NM_144606.7:c.86T>C