Canonical Allele Identifier: PA2827722025
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1470326
ClinVar RCV Id: RCV001973242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser296Thr
CA398533085
NM_001353231.2:c.886T>A