Canonical Allele Identifier: PA2827720921
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 184619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro428His
CA189480
NM_001353230.2:c.1283C>A