Canonical Allele Identifier: PA2827721312
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1729958
ClinVar RCV Id: RCV002326214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Cys11Tyr
CA398535467
NM_001353231.2:c.32G>A