Allele Registry

Canonical Allele Identifier: PA2499251421

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV001350360

ClinVar Variation:

1045881

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Ala463Pro	CA398531442 NM_001353229.2:c.1387G>C