Allele Registry

Canonical Allele Identifier: PA2827719982

Gene: FLCN HGNC NCBI

ClinVar Allele:

138162

ClinVar RCV:

RCV000121099

RCV000163762

RCV000543424

RCV000765335

RCV003952599

ClinVar Variation:

134423

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340159.1:p.Ala45Gly	CA159761 NM_001353230.2:c.134C>G