Allele Registry

Canonical Allele Identifier: PA2830284102

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV002450163

RCV003607544

ClinVar Variation:

1790269

HGVS (amino-acid)	Matching Registered Transcripts
NP_653207.1:p.Ser79Leu	CA398535039 NM_144606.7:c.236C>T