Canonical Allele Identifier: PA2827719962
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409391
ClinVar RCV Id: RCV000469363 RCV001017432 RCV001558005 RCV001844165 RCV002489056 RCV003409629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ser38Ile
CA8416514
NM_001353230.2:c.113G>T