Canonical Allele Identifier: PA2827721272
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 653717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro572His
CA398529794
NM_001353230.2:c.1715C>A