Canonical Allele Identifier: PA2827720915
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 566387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro427Leu
CA288307171
NM_001353230.2:c.1280C>T