Canonical Allele Identifier: PA2499297845
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1049988
ClinVar RCV Id: RCV001356755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser68Asn
CA398535110
NM_144997.7:c.203G>A