Allele Registry

Canonical Allele Identifier: PA2827721508

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV002450163

RCV003607544

ClinVar Variation:

1790269

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340160.1:p.Ser79Leu	CA398535039 NM_001353231.2:c.236C>T