Canonical Allele Identifier: PA2827720661
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro326Leu
CA8416182
NM_001353230.2:c.977C>T