Canonical Allele Identifier: PA645426389
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409391
ClinVar RCV Id: RCV000469363 RCV001017432 RCV001558005 RCV001844165 RCV002489056 RCV003409629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser38Ile
CA8416514
NM_144997.7:c.113G>T