Allele Registry

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Canonical Allele Identifier: PA658664469

Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485587

ClinVar RCV Id: RCV000562286 RCV000687129 RCV003478284

ClinVar Variation Id: 1000495

ClinVar RCV Id: RCV001296639

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Gly319Arg	CA8416188 NM_144997.7:c.955G>C CA398532928 NM_144997.7:c.955G>A