Canonical Allele Identifier: PA2827720922
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro428Leu
CA159789
NM_001353230.2:c.1283C>T